TABLE 2.
MICs of meropenem and conjugation efficiency in transformants with plasmids from representative isolates in each groupa
| Original species | Group | Original host isolate | MIC (mg/liter) | Avg conjugation efficiency ± SD |
|---|---|---|---|---|
| E. coli | pKPI-6 | E174 | 4 | (8.1 ± 3.8) × 10−2 |
| IncN | E066 | 16 | (2.2 ± 3.1) × 10−4 | |
| IncN | E033 | 16 | (2.4 ± 1.3) × 10−2 | |
| IncF | E305 | <1 | (7.5 ± 2.3) × 10−4 | |
| K. pneumoniae | pKPI-6 | E188 | 4 | (3.7 ± 2.0) × 10−1 |
| IncN | E187 | 4 | (2.9 ± 1.1) × 10−1 | |
| IncN | E196 | 16 | (4.4 ± 3.5) × 10−1 | |
| Non-IncN KP | E208 | 4 | 0 | |
| Non-IncN KP | E328 | 2 | (3.1 ± 2.6) × 10−4 |
Groups correspond to those in Fig. 1. Plasmids from representative isolates in each group were transformed into E. coli TOP10 strain by electroporation. MICs of meropenem for these transformants were measured by the broth microdilution method, in triplicate. The conjugation assay was conducted by mating the transformants as donors and E. coli TUM3456 as a recipient. The conjugation frequency was calculated as the CFU number of transconjugants per number of donors plus transconjugants. Average conjugation efficiencies from triplicate assays are indicated.